Literature DB >> 30622218

Myogenin promoter-associated lncRNA Myoparr is essential for myogenic differentiation.

Keisuke Hitachi1, Masashi Nakatani1, Akihiko Takasaki2, Yuya Ouchi3, Akiyoshi Uezumi1, Hiroshi Ageta1, Hidehito Inagaki3, Hiroki Kurahashi3, Kunihiro Tsuchida4.   

Abstract

Promoter-associated long non-coding RNAs (lncRNAs) regulate the expression of adjacent genes; however, precise roles of these lncRNAs in skeletal muscle remain largely unknown. Here, we characterize a promoter-associated lncRNA, Myoparr, in myogenic differentiation and muscle disorders. Myoparr is expressed from the promoter region of the mouse and human myogenin gene, one of the key myogenic transcription factors. We show that Myoparr is essential both for the specification of myoblasts by activating neighboring myogenin expression and for myoblast cell cycle withdrawal by activating myogenic microRNA expression. Mechanistically, Myoparr interacts with Ddx17, a transcriptional coactivator of MyoD, and regulates the association between Ddx17 and the histone acetyltransferase PCAF Myoparr also promotes skeletal muscle atrophy caused by denervation, and knockdown of Myoparr rescues muscle wasting in mice. Our findings demonstrate that Myoparr is a novel key regulator of muscle development and suggest that Myoparr is a potential therapeutic target for neurogenic atrophy in humans.
© 2019 The Authors.

Entities:  

Keywords:  DEAD box protein; chromatin; myogenesis; transcriptional regulation

Mesh:

Substances:

Year:  2019        PMID: 30622218      PMCID: PMC6399612          DOI: 10.15252/embr.201847468

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


  61 in total

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  22 in total

1.  Long noncoding RNA pncRNA-D reduces cyclin D1 gene expression and arrests cell cycle through RNA m6A modification.

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2.  Upregulated miR-9-5p inhibits osteogenic differentiation of bone marrow mesenchymal stem cells under high glucose treatment.

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4.  Data describing the effects of depletion of Myoparr, myogenin, Ddx17, and hnRNPK in differentiating C2C12 cells.

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